Canonical Allele Identifier: CA2091591574
Gene: NEK5 HGNC NCBI
ALG11 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.52035189A= , CM000675.2:g.52035189A= GRCh38
NC_000013.10:g.52609325A= , CM000675.1:g.52609325A= GRCh37
NC_000013.9:g.51507326A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000647945.2:c.*1759T= (NEK5) ENSP00000497892.1:n.*1759T=
ENST00000684899.1:c.*1759T= (NEK5) MANE Select ENSP00000509632.1:n.*1759T=
ENST00000649708.2:c.275+16046A= (ALG11) ENSP00000497459.2:n.275+16046A=
ENST00000652502.1:n.3921T= (NEK5)
ENST00000679495.1:n.44+22727A= (ALG11)
ENST00000529080.5:n.2462T= (NEK5)
NM_001365552.1:c.*1759T= (NEK5) MANE Select NP_001352481.1:n.*1759T=
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